Bromelain induces cardioprotection against ischemia-reperfusion injury through Akt/FOXO pathway in rat myocardium
Autor: | Roger S. Thrall, Utpal Raychaudhuri, Venugopal P. Menon, Mahesh Thirunavukkarasu, Bela Juhasz, Lijun Zhan, Rima Pant, Hajime Otani, Nilanjana Maulik, Sapna Srivastava, Suresh Varma Penumathsa, Eric R. Secor |
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Rok vydání: | 2008 |
Předmět: |
Male
medicine.medical_specialty Cardiotonic Agents Bromelain (pharmacology) Physiology Blood viscosity Myocardial Infarction Ischemia Apoptosis Myocardial Reperfusion Injury In Vitro Techniques Pharmacology Article Ventricular Function Left Rats Sprague-Dawley Cytosol Heart Rate Coronary Circulation Physiology (medical) Internal medicine Animals Medicine Phosphorylation Protein kinase B Cardioprotection business.industry Myocardium Gyógyszerészeti tudományok Anti-Inflammatory Agents Non-Steroidal Proteolytic enzymes Nuclear Proteins Forkhead Transcription Factors Orvostudományok medicine.disease Bromelains Rats Endocrinology Heart Function Tests Cardiology and Cardiovascular Medicine business Proto-Oncogene Proteins c-akt Reperfusion injury Signal Transduction |
Zdroj: | American Journal of Physiology-Heart and Circulatory Physiology. 294:H1365-H1370 |
ISSN: | 1522-1539 0363-6135 |
DOI: | 10.1152/ajpheart.01005.2007 |
Popis: | Bromelain (Br), a proteolytic enzyme extracted from the stem of the pineapple, is known to possess anti-inflammatory activity and has been shown to reduce blood viscosity, prevent the aggregation of blood platelets, and improve ischemia-reperfusion (I/R) injury in a skeletal muscle model. We investigated the capacity of Br to limit myocardial injury in a global I/R model. Adult male Sprague-Dawley rats were divided into two groups: control (PBS) and Br at 10 mg/kg in PBS administered via intraperitoneal injection (twice/day) for 15 consecutive days. On day 16, the hearts were excised and subjected to 30 min of global ischemia followed by 2 h of reperfusion. Br treatment showed higher left ventricular functional recovery throughout reperfusion compared with the controls [maximum rate of rise in intraventricular pressure (dP/d tmax), 2,225 vs. 1,578 mmHg/s at 2 h reperfusion]. Aortic flow was also found to be increased in Br treatment when compared with that in untreated rats (11 vs. 1 ml). Furthermore, Br treatment reduced both the infarct size (34% vs. 43%) and the degree of apoptosis (28% vs. 37%) compared with the control animals. Western blot analysis showed an increased phosphorylation of both Akt and FOXO3A in the treatment group compared with the control. These results demonstrated for the first time that Br triggers an Akt-dependent survival pathway in the heart, revealing a novel mechanism of cardioprotective action and a potential therapeutic target against I/R injury. |
Databáze: | OpenAIRE |
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